4829-04-3 Usage
Uses
Used in Chemical Synthesis:
1,3-Dithiolane is used as a synthetic building block for the creation of various sulfur-containing heterocyclic compounds. Its unique structure and reactivity make it a valuable component in the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
1,3-Dithiolane is used as a key intermediate in the synthesis of pharmaceutical compounds. Its sulfur-containing structure can be exploited to design and develop new drugs with improved properties, such as enhanced bioavailability, selectivity, and potency.
Used in Material Science:
1,3-Dithiolane can be utilized as a component in the development of novel materials with specific properties, such as improved conductivity, stability, or reactivity. Its incorporation into polymers or other materials can lead to the creation of advanced materials for various applications, including electronics, energy storage, and environmental protection.
Used in Analytical Chemistry:
1,3-Dithiolane can be employed as a reference compound or a reagent in analytical chemistry, particularly in the study of electron-impact fragmentation patterns. Its well-defined structure and known fragmentation modes make it a useful tool for understanding the behavior of similar compounds under various analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 4829-04-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4829-04:
(6*4)+(5*8)+(4*2)+(3*9)+(2*0)+(1*4)=103
103 % 10 = 3
So 4829-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H6S2/c1-2-5-3-4-1/h1-3H2
4829-04-3Relevant academic research and scientific papers
Novel 1,5,3-dithiazepanes: Three-component synthesis, stereochemistry, and fungicidal activity
Akhmetova,Murzakova,Tyumkina,Khabibullina,Bushmarinov,Korzhova,Galimzyanova
, p. 2140 - 2148 (2013/10/01)
Three-component heterocyclization of hydrazine with formaldehyde and ethane-1,2-dithiol gave previously unknown 3,3′-bi(1,5,3-dithiazepane). Its stereochemistry was determined by X-ray diffraction. The reaction with higher aliphatic aldehydes RCHO (R = Me
HOMOLYTIC LIQUID-PHASE TRANSFORMATIONS OF 2-ETHOXY-1,3-DITHIOLANE AND 2-ETHOXY-1,3-OXATHIOLANE
Batyrbaev, N. A.,Zorin, V. V.,Zlotskii, S. S.,Rakhmankulov, D. L.
, p. 1369 - 1371 (2007/10/02)
The direction of the homolytic transformations in 2-ethoxy-1,3-dithiolane and 2-ethoxy-1,3-oxathiolane was investigated. 1,3-Dithiolane and 1,3-dithiolan-2-one are formed from 2-ethoxy-1,3-dithiolane, and 1,3-oxathiolane-2-one, 1,3-oxathiolane, ethyl thioformate, and diethyl monothiocarbonate are formed from 2-ethoxy-1,3-oxathiolane.The temperature dependence of the yield and ratio of the reaction products was determined.
